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The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

ADF8 and ADF11 help root hairs grow by responding to hormones and environmental signals.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

VILLIN4 helps root hair growth by organizing actin with calcium.

The PIRL laser cuts tissue with less damage and scarring than traditional methods.

Hair graying is caused by damage and cell depletion but might be temporarily reversible with drugs and hormones.

Ritlecitinib effectively treats severe Alopecia Areata by reducing harmful immune activity in the skin.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Nrf2 helps protect skin from damage but too much can cause skin problems.

Activating Nrf2 can improve wound healing by increasing hair follicle stem cells.

Certain immune cells worsen post-surgery gut paralysis by activating a specific immune response.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Id2 gene helps keep hair follicle stem cells inactive.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.

IL-18 signaling helps mature Tregs move into the thymus.

Red light exposure slows aging in mice by improving fat metabolism.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

The study created special nanoparticles that effectively deliver an anti-inflammatory drug to treat skin inflammation in psoriasis.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

Tofacitinib can cause a rare rash called SDRIFE, which resolves after stopping the drug.